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[重症肌无力家族型的临床分析]

[Clinical analysis of familial forms of myasthenia].

作者信息

Strokov I A, Verbitskiĭ A M, Kvirkveliia N B, Gekht B M

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1986;86(3):321-6.

PMID:3705835
Abstract

Having studied 29 cases of myasthenia observed in 12 families, as well as 578 relatives of 59 patients with myasthenia, the authors have identified clinical characteristics of familial forms of myasthenia and the frequency of familial myasthenia among patient's relatives. It has been shown that familial forms of myasthenia are characterized by the appearance of a number of symptoms that are not typical of the common sporadic forms of myasthenia, which indicates the involvement, in addition to synaptic structures, of distal portions of peripheral nerves and/or muscle fibers. In families of myasthenic patients there is an extremely high rate of collagenoses, allergic diseases, diabetes, thyroid disease and malignant tumors.

摘要

在对12个家族中观察到的29例肌无力病例以及59例肌无力患者的578名亲属进行研究后,作者确定了家族性肌无力的临床特征以及患者亲属中家族性肌无力的发生率。结果表明,家族性肌无力的特征是出现一些常见散发性肌无力形式所不具有的症状,这表明除了突触结构外,外周神经远端部分和/或肌纤维也受到了影响。在肌无力患者的家族中,胶原病、过敏性疾病、糖尿病、甲状腺疾病和恶性肿瘤的发病率极高。

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